Variant report

Variant	rs7677036
Chromosome Location	chr4:88304115-88304116
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:88303180..88304947-chr4:88309411..88311690,2	K562	blood:
2	chr4:88303146..88304947-chr4:88309411..88312436,3	K562	blood:
3	chr4:88302651..88305218-chr4:88310752..88312524,2	MCF-7	breast:
4	chr4:88299456..88302215-chr4:88302964..88305080,2	K562	blood:
5	chr4:88302371..88304822-chr4:88310652..88313437,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000198189	Chromatin interaction

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs11097148	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11722370	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11727469	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11945520	1.00[CHB][hapmap]
rs4305486	1.00[CHB][hapmap]
rs4435709	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4585263	0.91[CEU][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4635784	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55721398	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55806847	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56156416	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56354112	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56878407	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs57124432	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61376571	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62319098	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62319099	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62319100	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62319101	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62319102	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62319103	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62319104	0.95[EUR][1000 genomes]
rs62319105	0.95[EUR][1000 genomes]
rs62319109	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62319110	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6531974	1.00[CHB][hapmap]
rs6531985	0.91[CEU][hapmap];1.00[CHB][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs66699153	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs67026749	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6811010	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs6817185	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6817242	0.87[CEU][hapmap];1.00[CHB][hapmap];0.97[YRI][hapmap];0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6818142	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6833678	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6834947	1.00[CHB][hapmap]
rs6839488	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6839620	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6840102	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6840247	0.91[CEU][hapmap];1.00[CHB][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6846149	1.00[CHB][hapmap]
rs6849382	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6849846	0.91[CEU][hapmap];1.00[CHB][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6850337	1.00[CHB][hapmap]
rs7661455	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7662471	1.00[CHB][hapmap]
rs7664479	1.00[CHB][hapmap]
rs7668285	1.00[CHB][hapmap]
rs7676494	1.00[CHB][hapmap]
rs7682516	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7682892	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7697960	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9684766	0.91[CEU][hapmap];1.00[CHB][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9684778	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1004518	chr4:88218473-88354403	Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv1002789	chr4:88239340-88606485	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:88254800-88311800	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr4:88256200-88310600	Weak transcription	Right Ventricle	heart
3	chr4:88257800-88311800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr4:88267400-88308000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr4:88267800-88306000	Weak transcription	Fetal Brain Female	brain
6	chr4:88276200-88311400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr4:88287400-88308000	Weak transcription	Spleen	Spleen
8	chr4:88290400-88305600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr4:88291000-88306000	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr4:88291000-88309000	Weak transcription	Right Atrium	heart
11	chr4:88293000-88304800	Weak transcription	Brain Germinal Matrix	brain
12	chr4:88293000-88306800	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr4:88293000-88307200	Weak transcription	Pancreas	Pancrea
14	chr4:88293000-88307600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr4:88293000-88308000	Weak transcription	Colonic Mucosa	Colon
16	chr4:88293000-88308800	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr4:88293000-88309600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr4:88293000-88311200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr4:88293200-88308000	Weak transcription	Left Ventricle	heart
20	chr4:88293200-88309600	Weak transcription	Brain Hippocampus Middle	brain
21	chr4:88293200-88309600	Weak transcription	Gastric	stomach
22	chr4:88293200-88311400	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr4:88293400-88304800	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr4:88293400-88308000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr4:88293400-88309800	Weak transcription	Brain Anterior Caudate	brain
26	chr4:88294000-88309400	Weak transcription	NHLF	lung
27	chr4:88294000-88309600	Weak transcription	Colon Smooth Muscle	Colon
28	chr4:88294000-88311000	Weak transcription	HSMM	muscle
29	chr4:88294200-88304800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr4:88294200-88307200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
31	chr4:88294200-88310800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr4:88294600-88308000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr4:88294800-88308000	Weak transcription	Lung	lung
34	chr4:88294800-88309400	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr4:88295000-88305600	Weak transcription	Primary hematopoietic stem cells	blood
36	chr4:88295000-88305800	Weak transcription	Brain Angular Gyrus	brain
37	chr4:88295000-88308000	Weak transcription	Duodenum Smooth Muscle	Duodenum
38	chr4:88295200-88309400	Weak transcription	Stomach Smooth Muscle	stomach
39	chr4:88295400-88311200	Weak transcription	Aorta	Aorta
40	chr4:88296000-88308000	Weak transcription	Primary T helper cells PMA-I stimulated	--
41	chr4:88296200-88309000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr4:88297000-88308200	Weak transcription	Hela-S3	cervix
43	chr4:88297400-88304600	Strong transcription	Primary monocytes fromperipheralblood	blood
44	chr4:88297400-88308200	Weak transcription	Rectal Smooth Muscle	rectum
45	chr4:88297400-88309400	Weak transcription	Brain Substantia Nigra	brain
46	chr4:88297400-88309600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr4:88297400-88309600	Weak transcription	A549	lung
48	chr4:88297400-88310000	Weak transcription	NHDF-Ad	bronchial
49	chr4:88297400-88310600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr4:88297400-88310800	Weak transcription	Osteobl	bone

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